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Research Coordinator

Sidra Medicine
QAT
Full-time
Junior · 2+ years experience
Onsite
Discovered 1 months ago
Communication

Full Job Posting

Qualifications

  • ESSENTIAL PREFERRED EducationBachelor’s Degree in medicine, natural sciences or other relevant field Experience
  • 2+ years’ experience in clinical research and/ or clinical research coordination
  • Experience with patients
  • Exceptions to the experience requirement may be granted for Qatari nationals (internal and external candidates), with a reduction of up to two (2) years. [For a DHP licensable role, the experience requirements mandated by the Department of Healthcare Professions, along with the defined scope of practice, must be strictly followed.]
  • Experience with local patientsJob Specific Skills and Abilities
  • Proven ability to maintain confidentiality
  • Demonstrated excellent communication skills
  • Proven electronic documentation, archiving and organizational skills
  • Proficiency with Microsoft Office suite
  • Fluency in written and spoken English
  • Arabic speaker

Responsibilities

  • Provides coordination for the investigator’s research projects involving liaison with stakeholders and core facilities.
  • Coordinates recruitment of patients and collects informed consents, assents, questionnaires and related documents.
  • Coordinates samples collection and transportation.
  • Manages the order of reagents/consumables/other items required for the projects.
  • Uses, maintains and organizes a database/folders containing patient information (including secured data and unidentified data, as relevant.
  • Manages the Case Report Forms, according to the different clinical research studies.
  • Adheres to Sidra’s standards as they appear in the Code of Conduct and Conflict of Interest policies
  • Adheres to and promotes Sidra’s Values
  • In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary.

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